Production of chlorine-containing copper phthalocyanines

ABSTRACT

CHLORINE-CPMTAINING PIGMENTARY COPPER PHTHALOCYANINES ARE PREPARED VIA THE PHTHALONITRILE SYNTHESIS USING AS THE SOLVENT A MEMBER FROM A SPECIFIED GROUP OF ORGANIC SULFONES. THE PRODUCT MAY BE USED AS SUCH OR AS A STABILIZER FOR CHLORINE-FREE COPPER PHTHALOCYANINE PIGMENT.

United States Patent O 3,834,922 PRODUCTION OF CHLORINE-CONTAININGCOPPER PHTHALOCYANINES Edward E. Jalfe, Union, N.J., assignor to E. I.du Pont de Nemours and Company, Wilmington, Del.

No Drawing. Original application Nov. 11, 1971, Ser. No. 197,978, nowPatent No. 3,770,765. Divided and this application July 2, 1973, Ser.No. 375,942

Int. Cl. C08h 17/14 US. Cl. 106-288 Q 2 Claims ABSTRACT OF THEDISCLOSURE Chlorine-containing pigmentary copper phthalocyanines areprepared via the phthalonitrile synthesis using as the solvent a memberfrom a specified group of organic sulfones. The product may be used assuch or as a stabilizer for chlorine-free copper phthalocyanine pigment.

Cross Reference to Related Application This application is a division ofapplication Ser. No. 197,978 filed Nov. 11, 1971, now US. Pat.3,770,765.

BACKGROUND OF THE INVENTION British Pat. 1,073,348 describes a techniquefor the direct manufacture of pigmentary chlorinated copperphthalocyanines by reacting a phthalonitrile, cupric chloride, and atertiary aromatic amine in nitrobenzene as an inert solvent. While thetechnique would appear to be most attractive in that the need for aparticle size reduction step is obviated, the use of a solvent havingsuch a strong characteristic odor combined with a low degree of watersolubility presents extreme difiiculties for a commerical operation.Attempts have been made to operate such a process using solvents otherthan nitrobenzene, but these have, as noted in the British patent, beenunsuccessful in that a pigmentary reaction product does not result.

SUMMARY OF THE INVENTION 'In accordance with the present invention ithas been found that the aforementioned disadvantages associated with thedirect production of a chlorine-containing pigmentary copperphthalocyanine via the phthalonitrile synthesis are overcome by carryingout the reaction in a solvent medium which is a dialkyl sulfone of 2-4carbon atoms or a cyclic sulfone of the formula C(CHM wherein n is aninteger of 4-5. Especially preferred solvents for use in accordance withthe invention are tetramethylene sulfone and dimethyl sulfone.

The utility of the particular sulfone solvents leading to the directproduction of chlorinated copper phthalocyanine is surprising sincenumerous other commercial solvents, including various highly polarsolvents as well, fail to yield pigmentary products when used in asimilar way.

It is a further finding of the invention that a chlorinefree copperphthalocyanine pigment can be stabilized against particle growth by thepresence therein of 5-25 weight percent, based on the chlorine-freephthalocyanine pigment, of a product synthesized in accordance with theaforementioned process using one of the specified organic sulfones asthe solvent. The stability of such a product is still further enhancedif it additionally contains 2-20 weight percent, based on thechlorine-free phthalocyanine pigment, of a calcium rosinate.

Patented Sept. 10, 1974 ice A number of significant processing andproduct advantages accrue with the utilization of the above describedclass of organic sulfones as solvents in which to effect the reactionbetween a phthalonitrile, a cupric chloride and a tertiary aromaticamine so as to produce a chlorinated copper phthalocyanine. On the onehand these organic sulfones are generally free of an objectionable odorand tend to be highly miscible with water, so that recovery of thechlorinated copper phthalocyanine products is greatly facilitated. Inaddition to the fact that pigmentary products are obtained directly, theproducts themselves are also crystal stable and highly resistant toflocculation when used in coating compositions, equalling or in somecases exceeding in these respects commercial grades of copperphthalocyanine pigments prepared using ordinary particle size reductiontechniques.

As above described, the organic solvents employed in accordance with theinvention for carrying out a reaction between a phthalonitrile, cupricchloride and a tertiary aromatic amine are either (a) dialkyl sulfonesof 2-4 carbon atoms, such as dimethyl sulfone and diethyl sulfone, or(b) cyclic sulfones of the formula wherein n is an integer of 4 to 5,thus tetramethylene sulfone or pentamethylene sulfone. It is significantthat diphenyl sulfone fails to directly yield pigmentary chlorinatedcopper phthalocyanine by the same reaction.

While in general it is preferred to carry out the reaction of theinvention using unsubstituted phthalonitrile so as to produce partiallychlorinated copper phthalocyanines of 3 to 7 weight percent chlorine,i.e., monochloro copper phthalocyanine, it is entirely practicable touse phthalonitriles having 1 to 4 chlorine atoms per molecule to producethe more highly chlorinated species.

The tertiary aromatic amine reactant should, in respect of the tertiarynitrogen, be relatively free from steric hindrance. For this reason itis desired that the tertiary aromatic amine should be one in which thecarbon atoms adjacent the tertiary nitrogen and not a part of a fusedring are free of substituents. Pyridine and quinoline are particularlyuseful examples of tertiary aromatic amines that may be so employed.

The use of cupric chloride is necessary for the direct attainment of achlorinated copper phthalocyanine in a pigmentary form according to theinvention. Cuprous chloride may be substituted in part but the majormolar proportion of the total copper salts so employed should besupplied by the cupric chloride. The utilization of hydrated coppersalts, indeed the presence of water in any form in the reaction mixture,should be avoided as such will tend to cause formation of non-pigmentaryproducts.

Ammonium molybdate is a known catalyst for the phthalonitrile synthesisbut its use in the present invention is wholly unnecessary, apparentlybecause the tertiary aromatic amine functions in part as a catalyst.

In general it is advantageous to carry out the preparation of the copperphthalocyanine using a mole ratio of the phthalonitrile to tertiaryaromatic amine in the range of 4:1 to 35:1. The ratio of the cupricchloride, plus other copper salts if used, to phthalonitrile should beat least about stoichiometric, i.e., 1 to 4 as usual, although an excessof the former is not objectionable and will generally tend to providehigher yields. The proportion of organic sulfone solvent in the reactionmixture is not critical to the reaction as such, although some losses inyield may be noted if unduly high or low amounts are used.

Temperatures as low as C. are operable for the production of thechlorine-containing copper phthalocyanines in accordance with theinvention, but it is generally preferable in order to achievesatisfactory yields of product that the reaction be performed attemperatures on the order of 170 to 190 C. Temperatures as high as 300C. may be used but some weakening of product strength may be noted. Aslittle as one-half hour at the required temperature can give good yieldsof pigmentary products but the preferred reaction time is on the orderof l to 4 hours.

The chlorine-containing copper phthalocyanine products of the invention,of course, may be used as such for the coloring of paints, plastics,films and the like. They are also useful, however, in the stabilizationof chlorinefree copper phthalocyanine pigments, either of the u or [3form, such as those typically produced by the phthalic anhydride/ureasynthesis. For this purpose it is preferable to employ 5 to 25 weightpercent, based on the chlorine-free copper phthalocyanine pigment, ofthe reaction product. A further enhancement in stability is obtainableif there is also included in the composition 2 to 20 weight percent,based on the chlorine-free copper phthalocyanine, of a calcium rosinatesuch as the calcium salt of hydrogenated rosin. It is merely necessaryto combine the components in the desired proportions, e.g. by standardball milling procedures, in order to effect the stabilization.

The following examples illustrate the invention and the advantagesthereof. Parts and percentages are by weight unless otherwise indicated.

Example 1 Into a round-bottom flask equipped with an agitator,thermometer, and drying tube, the following chemicals are charged:

125 mls. tetramethylene sulfone,

16 grams (0.125 mole) phthalonitrile,

8.8 grams (0.0654 mole) anhydrous CuCI and 1.25 grams (0.0158 mole)pyridine.

The mass is stirred and, over a period of about one-half hour, is thenheated to 180190 C. This temperature is maintained for about five hours.During the heat-up period, at one point the solids are nearly insolution and copper phthalocyanine begins to form when the temperaturereaches about 160 C. The reaction mixture is then cooled to about 40 C.

The cooled mixture is diluted with 200 ml. methanol and stirred untiluniform. The product is recovered by filtration, washed with somealcohol and then washed with water until chloride-free. The product isdried at 85 C. and is found to weigh 16.4 grams.

On analysis the pigmentary product shows 6.99% chlorine. By X-raydiffraction analysis, the crystal form is shown to be gamma monochlorocopper phthalocyanine.

The pigment is rated excellent in terms of strength, intensity andflocculation resistance. In these respects it compares favorably to acommercial copper phthalocyanine pigment of similar chlorine content.

Example 2 The procedure of Example 1 is followed through the firstparagraph thereof, i.e. through the point of cooling the reactionmixture to 40 C. The mixture is then diluted with a solution of ml.concentrated H 50 in one liter of water and the resulting suspensionboiled with open steam for one-half hour. The hot suspension is filteredand the solid is washed with hot water until free of acid and chloride.After drying at 82 C., the yield is 15.5 g. The chlorine centent in theproduct is 6.1%. The product shows essentially the same characteristicsas that of Example 1.

Example 3 Following the same procedure as given in Example 1, exceptusing only half the amount of CuCl (i.e. 4.4 g.= 0.0327 mole), 10.5grams of pigmentary product is obtained having a chlorine content of3.4%. In terms of pigmenting strength the resulting product is superiorto a commercially available semichloro copper phthalocyanine noted forgood texture characteristics.

Example 4 This example shows that the sequence of ingredient additioncan be changed without significant effect on quality or yield.

In a round-bottom flask,

ml. tetramethylene sulfone,

4.4 grams (0.0327 mole) anhydrous cupric chloride, and

1.25 ml. (0.0158 mole) pyridine This example shows the use of quinolineas the tertiary base in the synthesis. The following ingredients aremixed in a round-bottom flask and stirred and heated to 180- 190 C.:

125 ml. tetramethylene sulfone,

16 grams (0.125 mole) phthalonitrile,

8.8 grams (0.0654 mole) anhydrous cupric chloride, and 2.04 grams(0.0158 mole) quinoline.

When the temperature reaches ISO- C., the copper phthalocyanine productbegins to form. The synthesis is completed as in Example 1, to yield13.5 grams of pigmentary product having a chlorine content of 6.3%.

In an alkyd vehicle, the product shows strength comparable to standardpigmentary products.

The pigment prepared according to this example, although not as strongin tinctorial properties, is of softer texture than thepyridine-catalyzed product of Examples 1 through 3. The product preparedusing quinoline, as in this example, is especially suitable, therefore,for use in pigmentation of plastics such as polyvinyl chloride.

Example 6 In this example dimethyl sulfone is used as the reactiomedium. In a round-bottom flask 125 grams dimethyl sulfone (solid) isheated to 70 C., and to it is then added 8.8 grams 0.0654 mole)anhydrous cupric chloride and 1.25 grams (0.0158 mole) pyridine.

The mixture of ingredients is heated to 100-110 C. 1n order to melt thesulfone. At this time, 16 grams (0.125 mole) phthalonitrile is added andthe temperature raised, with stirring to 190 C. and maintained at thislevel for three and one-half hours. The mixture is then cooled to about80 C. and diluted with 200 ml. methanol. T0 dissolve the total amount ofsulfone, the mixture is subsequently washed with one and eight-tenthsliters of methanol and then with water until free of chloride. The yieldof pigmentary product is 15.4 grams and the chlorine content is 7.02%.The product is found to be more intense and stronger than a commercialsemichloro copper phthalocyanine.

Example 7 The preparation of polychloro copper phthalocyanine accordingto the process of the present invention is shown in this example.

5 The following ingredients are mixed in a round-bottom flask and heatedwith stirring to 180-190 C. over a onehalf hour period.

125 m1. tetramethylene sulfone 33.2 grams (0.125 mole)tetrachlorophthalonitrile 8.8 grams (0.0654 mole) anhydrous cupricchloride 1.25 grams (0.0158 mole) pyridine The product begins to formwhen the temperature reaches 180 C. The temperature is maintained atISO-190 C. for three and one-half hours, and the product is recoveredand washed according to the procedure of Example 1. Yield of pigment is22.9 grams and the chlorine content is about 50%. The pigmentary productis as strong as a commercial polychloro copper phthalocyanine but isless intense. It is identical to a commercial polychloro copperphthalocyanine product in its infra-red spectrum and Y-ray diffractionpattern.

Example 8 What is claimed is:

1. As a novel product, a chlorine-free copper phthalocyanine pigmentstabilized by the presence in admixture therewith of 5-25 weightpercent, based on the phthalocyanine pigment, of the product obtained byreaction of a phthalonitrile containing 0-4 chlorine substituents,cupric chloride, and a tetriary aromatic amine in which the tertiarynitrogen is a part of the aromatic ring and in which carbon atomsadjacent the tertiary nitrogen and not a part of a fused ring are freeof substituents, at a temperature of 170-300 C. in an organic solventcomprising a dial kyl sulfone of 2-4 carbon atoms or a cyclic sulfone ofthe formula References Cited UNITED STATES PATENTS 6/1962 Bro uillard etal. 106-288 Q 11/1973 Jafie 260-3l4.5

DELBERT E. GANTZ, Primary Examiner J. V. HOWARD, Assistant Examiner US.Cl. X.R. 106308 Q

